Estimates of all cause mortality and cause specific mortality associated with proton pump inhibitors among US veterans: cohort study

被引:152
作者
Xie, Yan [1 ,2 ]
Bowe, Benjamin [1 ,3 ]
Yan, Yan [1 ,4 ]
Xian, Hong [1 ,3 ]
Li, Tingting [1 ,5 ]
Al-Aly, Ziyad [1 ,2 ,5 ,6 ,7 ]
机构
[1] St Louis Hlth Care Syst, Dept Vet Affairs, Clin Epidemiol Ctr, 915 North Grand Blvd, St Louis, MO 63106 USA
[2] Vet Res & Educ Fdn St Louis, St Louis, MO 63103 USA
[3] St Louis Univ, Dept Biostat, Coll Publ Hlth & Social Justice, St Louis, MO 63103 USA
[4] Washington Univ, Sch Med, Dept Surg, Div Publ Hlth Sci, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[6] St Louis Hlth Care Syst, Med Serv, Dept Vet Affairs, Renal Sect, St Louis, MO 63106 USA
[7] Washington Univ, Sch Med, Inst Publ Hlth, St Louis, MO 63130 USA
来源
BMJ-BRITISH MEDICAL JOURNAL | 2019年 / 365卷
关键词
DIMENSIONAL PROPENSITY SCORE; DENSITY-LIPOPROTEIN CHOLESTEROL; KIDNEY-FUNCTION; HEME OXYGENASE-1; GASTRIC-CANCER; INCREASED RISK; DISEASE; DRUGS; COMPLICATIONS; ADJUSTMENT;
D O I
10.1136/bmj.l1580
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To estimate all cause mortality and cause specific mortality among patients taking proton pump inhibitors (PPIs). DESIGN Longitudinal observational cohort study. SETTING US Department of Veterans Affairs. PARTICIPANTS New users of PPIs (n=157 625) or H2 blockers (n=56 842). MAIN OUTCOME MEASURES All cause mortality and cause specific mortality associated with taking PPIs (values reported as number of attributable deaths per 1000 patients taking PPIs). RESULTS There were 45.20 excess deaths (95% confidence interval 28.20 to 61.40) per 1000 patients taking PPIs. Circulatory system diseases (number of attributable deaths per 1000 patients taking PPIs 17.47, 95% confidence interval 5.47 to 28.80), neoplasms (12.94, 1.24 to 24.28), infectious and parasitic diseases (4.20, 1.57 to 7.02), and genitourinary system diseases (6.25, 3.22 to 9.24) were associated with taking PPIs. There was a graded relation between cumulative duration of PPI exposure and the risk of all cause mortality and death due to circulatory system diseases, neoplasms, and genitourinary system diseases. Analyses of subcauses of death suggested that taking PPIs was associated with an excess mortality due to cardiovascular disease (15.48, 5.02 to 25.19) and chronic kidney disease (4.19, 1.56 to 6.58). Among patients without documented indication for acid suppression drugs (n= 116 377), taking PPIs was associated with an excess mortality due to cardiovascular disease (22.91, 11.89 to 33.57), chronic kidney disease (4.74, 1.53 to 8.05), and upper gastrointestinal cancer (3.12, 0.91 to 5.44). Formal interaction analyses suggested that the risk of death due to these subcauses was not modified by a history of cardiovascular disease, chronic kidney disease, or upper gastrointestinal cancer. Taking PPIs was not associated with an excess burden of transportation related mortality and death due to peptic ulcer disease (as negative outcome controls). CONCLUSIONS Taking PPIs is associated with a small excess of cause specific mortality including death due to cardiovascular disease, chronic kidney disease, and upper gastrointestinal cancer. The burden was also observed in patients without an indication for PPI use. Heightened vigilance in the use of PPI may be warranted.
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页数:13
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